Solutions for Chapter 2.13: The C5H12 Isomers

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Full solutions for Organic Chemistry, | 9th Edition

ISBN: 9780073402741

Organic Chemistry, | 9th Edition | ISBN: 9780073402741 | Authors: Francis A Carey Dr., Robert M. Giuliano

Solutions for Chapter 2.13: The C5H12 Isomers

Solutions for Chapter 2.13
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This textbook survival guide was created for the textbook: Organic Chemistry, , edition: 9. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 2.13: The C5H12 Isomers includes 1 full step-by-step solutions. Organic Chemistry, was written by Patricia and is associated to the ISBN: 9780073402741. Since 1 problems in chapter 2.13: The C5H12 Isomers have been answered, more than 10707 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • acid-catalyzed hydration

    A reaction that achieves the addition of water across a double bond in the presence of an acid catalyst.

  • Antiaromatic compound

    A monocyclic compound that is planar or nearly so, has one 2p orbital on each atom of the ring, and has 4n p electrons in the cyclic arrangement of overlapping 2p orbitals, where n is an integer. Antiaromatic compounds are especially unstable

  • beta (b) anomer

    The cyclic hemiacetal of an aldose, in which the hydroxyl group at the anomeric position is cis to the CH2OH group.

  • cathode rays

    Streams of electrons that are produced when a high voltage is applied to electrodes in an evacuated tube. (Section 2.2)

  • cephalins

    Phosphoglycerides that contain ethanolamine.

  • chemical changes

    Processes in which one or more substances are converted into other substances; also called chemical reactions. (Section 1.3)

  • diffusion.

    The gradual mixing of molecules of one gas with the molecules of another by virtue of their kinetic properties. (5.7)

  • Eclipsed conformation

    A conformation about a carboncarbon single bond in which the atoms or groups on one carbon are as close as possible to the atoms or groups on an adjacent carbon.

  • entropy

    A thermodynamic function associated with the number of different equivalent energy states or spatial arrangements in which a system may be found. It is a thermodynamic state function, which means that once we specify the conditions for a system—that is, the temperature, pressure, and so on—the entropy is defined. (Section 19.2)

  • Grignard reagent

    A carbanion with the structure RMgX.

  • half-life

    The time required for the concentration of a reactant substance to decrease to half its initial value; the time required for half of a sample of a particular radioisotope to decay. (Sections 14.4 and 21.4)

  • linkage isomers

    Structural isomers of coordination compounds in which a ligand differs in its mode of attachment to a metal ion. (Section 23.4)

  • liquid

    Matter that has a distinct volume but no specific shape. (Section 1.2)

  • N-glycoside

    The product obtained when a monosaccharide is treated with an amine in the presence of an acid catalyst.

  • observed rotation

    The extent to which plane-polarized light is rotated by a solution of a chiral compound.

  • Photosensitizer

    A compound that absorbs light and transfers the energy to another molecule.

  • polysaccharide

    A substance made up of many monosaccharide units joined together. (Section 24.8)

  • silica

    Common name for silicon dioxide. (Section 22.4)

  • Williamson ether synthesis

    A general method for the synthesis of dialkyl ethers by an SN2 reaction between a haloalkane and an alkoxide ion.

  • Zwitterion

    An internal salt of an amino acid; the carboxylate is negatively charged, and the ammonium group is positively charged

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